Znn3bq.jpeg
±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 229  |  »Ø¸´: 1

1power1

ľ³æ (ÕýʽдÊÖ)

[ÇóÖú] Çó΢Æ×

11.1,11.1,16.4,17.7,18.4,18.8,19.9,20.8,21.7,26.7,29.6,31.8,31.9,35.9,38.0,38.2,39.2,41.6,42.3,42.6,53.5,54.7,66.5,72.4,74.7,116.3,131.0,134.2,142.8

ë®´úÂÈ·Â
л
»Ø¸´´ËÂ¥
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

kobechan

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

ʯ¹Ä

ÓÅÐã°æÖ÷

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
1power1: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-12 01:40:56
1 .     3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene
C30H52O3     ÏàËÆ¶È:93.3%
Zeitschrift f¨¹r Naturforschung C          2002          57          489-495
Microbial Transformation of a Mixture of Argentatin A and Incanilin
Key words: Argentatin A, Incanilin, Biotransformation
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËÆ¶È:86.2%
Phytochemistry          1999          51          891-898
Antitumor sterols from the mycelia of Cordyceps sinensis
Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cerevisterol
C28H44O3     ÏàËÆ¶È:82.7%
Chinese Traditional and Herbal Drugs          2009          40          1211-1214
Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿
ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     stellastero l
C28H46O     ÏàËÆ¶È:79.3%
Chinese Traditional and Herbal Drugs          2009          40          1211-1214
Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿
ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     cerevisterol
C28H46O3     ÏàËÆ¶È:79.3%
Chemistry of Natural Compounds          2011          47          858-861
Secondary metabolites of endophytic fungus Xylaria sp. YC-10 of Azadirachta indica
Shao-Hua Wu, You-Wei Chen and Cui-Ping Miao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (24S)-ergost-5-en-3¦Â,7b -diol
C28H48O2     ÏàËÆ¶È:72.4%
Chemical & Pharmaceutical Bulletin          2005          53(2)          168-171
New Sphingolipids and a Sterol from a Lobophytum Species of the Indian Ocean
Pendyala MURALIDHAR, Muthyala Muralikrishna KUMAR,Nallamothu KRISHNA,Chaganty Bheemasankara RAO, and Desaraju Venkata RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (22S,23S)-3¦Â,7¦Á-Dihydroxy-22,23-oxidostigmast-5-ene
C29H48O3     ÏàËÆ¶È:68.9%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (22S,23S)-3¦Â,7¦Â-Dihydroxy-22,23-oxidostigmast-5-ene
C29H48O3     ÏàËÆ¶È:68.9%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:68.9%
Chinese Traditional and Herbal Drugs          2010          41          187-190
Studies on chemical constituents of Oxytropis kansuensis
GONG Hong-fei; YANG Ai-mei; LIU Jun-xi; DI Duo-long
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ergosterol
C28H44O     ÏàËÆ¶È:68.9%
Chinese Traditional and Herbal Drugs          2009          40          1211-1214
Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿
ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ¶¹çÞ´¼-5,22-3¦Â,7¦Á-¶þ´¼
C29H50O     ÏàËÆ¶È:68.9%
Chinese Traditional and Herbal Drugs          2005          36          982-983
ÄϰåÀ¶¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÎâìÏÇï,Ç®±ó,ÕÅÈÙÆ½,×Þ³Î,Áõ¹â
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:68.9%
Chinese Journal of Medicinal Chemistry          2008          18          452-456
Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora
DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Homobrassinolide
C29H50O6     ÏàËÆ¶È:68.9%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     schleicheol 2
C30H52O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          72-78
Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1
George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     7¦Â-methoxy-sigmast-5-en-3¦Â-ol
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2008          33          1035-1038
Study on Steroids of Cacalia tangutica
LIU Qing, LIU Zhenling, TIAN Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3,3-(Ethylenedioxy)-7¦Â-hydroxy-5¦Á-cholestan-24-amine
C29H51NO3     ÏàËÆ¶È:65.6%
Steroids          2002          67          291-304
The synthesis of spermine analogs of the shark aminosterol squalamine
Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     24-methyl-7¦Á,8¦Á-epoxy-3¦Â,5¦Á,6¦Á-trihydroxycholest-22-ene
C28H46O4     ÏàËÆ¶È:65.5%
Journal of Natural Products          1996          59          679-682
Isolation of Polyhydroxysteroids from the Gorgonian Acabaria undulata
Jongheon Shin, Youngwan Seo, Jung-Rae Rho, and Ki Woong Cho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     7¦Â-Hydroxysitosterol
C29H50O2     ÏàËÆ¶È:65.5%
Journal of Chinese Pharmaceutical Sciences          2007          16          288-293
Chemical constituents of the flower buds of Tussilago farfara
Yu-Feng Liu; Xiu-Wei Yang and Bin Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (22R,23R)-3¦Â-Bromo-5¦Á,22,23-trihydroxystigmastan-6-one
C31H52O3Br     ÏàËÆ¶È:65.5%
Steroids          2000          65          329-337
Synthesis and bioactivity evaluation of brassinosteroid analogs
Javier A. Ram¨ªrez, Osvaldo M. Teme Centuri¨®n, Eduardo G. Gros, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2008          33          1566-1568
Studies on chemical constituents from stem bark of Trwia nudiflora
WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     stigmast 5-en-3¦Â,7¦Á-diol
C29H50O2     ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2008          33          1035-1038
Study on Steroids of Cacalia tangutica
LIU Qing, LIU Zhenling, TIAN Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ergost-5,22-dien-3¦Â,7¦Â-diol
C28H46O2     ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2005          36          510-511+550
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔÆ±£,ÂÞÏþ¶«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:65.5%
Chinese Journal of Natural Medicines          2007          5          105-107
Chemical Constituents of African Plant Harpagophytum procumbens
QI Jin; CHEN Ji-Jun; TU Ying; CHEN Lu; YU Bo-Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     7¦Â-hydroxysitosterol
    ÏàËÆ¶È:65.5%
Chinese Journal of Natural Medicines          2007          5          105-107
Chemical Constituents of African Plant Harpagophytum procumbens
QI Jin; CHEN Ji-Jun; TU Ying; CHEN Lu; YU Bo-Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:65.5%
Chinese Journal of Natural Medicines          2010          8          267-269
Steroids and Phenols from Sonchus arvensis
XIA Zheng-Xiang; LIANG Jing-Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     stigmast-5-ene-3¦Â-,7¦Â,15¦Á-triol
C29H50O3     ÏàËÆ¶È:65.5%
Pharmazie          2002          57          209-211
Two new steroids from Adenophora stenanthina subsp. xifengensis
Zhen-Fu Hou - Yong-Qiang Tu - Yu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     stigmast-5-en-3¦Â,7¦Á-diol
    ÏàËÆ¶È:65.5%
Pharmazie          2005          60          464-467
Steroids from Saussurea ussuriensis
Jia-Tao Feng and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     stigmast-5-en-3¦Â,7¦Á-diol
    ÏàËÆ¶È:65.5%
Chinese Pharmaceutical Journal          1999          34          366-367
Chemical constituents of Pugionium cornutum
Mei Shuangxi (Mei SX), Pan Xiaohui (Pan XH), Hou Zhenfu (Hou ZF), et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     7¦Â-hydroxys-itosterol
    ÏàËÆ¶È:65.5%
Chinese Pharmaceutical Journal          2008          43          897-899
Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook
WANG Yuan, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     24S-24-Methylcholest-5-ene-1¦Á,3¦Â-diol
C28H48O2     ÏàËÆ¶È:65.5%
Bulletin of the Chemical Society of Japan          2008          81          1616-1620
Anti-Inflammatory Polyoxygenated Steroids from the Soft Coral Sinularia sp.
Jui-Hsin Su, Ching-Li Lo, Yi Lu, Zhi-Hong Wen, Chiung-Yao Huang, Chang-Feng Dai, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-03-11 22:36:47
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ 1power1 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] »¯Ñ§¹¤³Ìµ÷¼Á289 +24 yangæÃ 2026-04-07 25/1250 2026-04-08 11:39 by Öí»á·É
[¿¼ÑÐ] 288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò +35 lllllos 2026-04-04 39/1950 2026-04-07 23:24 by Ò»Ö»ºÃ¹û×Ó?
[¿¼ÑÐ] 323Çóµ÷¼Á +3 ÁÖzlu 2026-04-07 4/200 2026-04-07 23:21 by lbsjt
[¿¼ÑÐ] ¿¼Ñе÷¼Á +8 ±ù±ù£¬£¬£¬ 2026-04-07 8/400 2026-04-07 22:49 by JourneyLucky
[¿¼ÑÐ] µ÷¼Á +18 ²»·ê´º 2026-04-05 19/950 2026-04-07 22:04 by lijunpoly
[¿¼ÑÐ] ×÷ÔÔ330µ÷¼Á +3 ÎÒÒªÉϺÃѧ 2026-04-02 4/200 2026-04-07 19:54 by biomichael
[¿¼ÑÐ] ²ÄÁÏÇóµ÷¼Á +18 Ò»ÑùYWY 2026-04-05 18/900 2026-04-07 15:49 by dxlg
[¿¼ÑÐ] 316Çóµ÷¼Á +7 yyxÏëµ÷¼Á 2026-04-05 7/350 2026-04-07 14:31 by shdgaomin
[¿¼ÑÐ] Ò»Ö¾Ô¸ÎäÀí³µÁ¾×¨Ë¶×Ü·Ö 281 Çóµ÷¼Á +4 Éϰ¶Ñо¿Éú. 2026-04-02 4/200 2026-04-07 09:52 by ¼ÓÓÍÏòδÀ´°¡
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +5 asdasdassda 2026-04-05 5/250 2026-04-06 09:32 by dongzh2009
[¿¼ÑÐ] Ò»Ö¾Ô¸ ½­ÄÏ´óѧ 085602 »¯¹¤×¨Ë¶ 338·ÖÇóµ÷¼Á +15 ·³ÕСç÷ 2026-04-05 15/750 2026-04-06 09:27 by cql1109
[¿¼ÑÐ] Ò»Ö¾Ô¸Çà¿Æ085500£¬³õÊÔ295·Ö£¬¹«¹²¿Î213·Ö +3 Óöµ½µÄÈËÔ¸Íû¶¼Ä 2026-04-05 3/150 2026-04-05 18:45 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ¿¼Ñе÷¼ÁÉúѰÕÒµ¼Ê¦ +3 ¹ËÕ°¿¼Ñа¡ 2026-04-05 3/150 2026-04-05 18:18 by à£à£à£0119
[¿¼ÑÐ] 282Çóµ÷¼Á +7 aaa³µÁ¾ 2026-04-02 11/550 2026-04-05 17:24 by yulian1987
[¿¼ÑÐ] 313Çóµ÷¼Á +3 º£ÈÕº£ÈÕ 2026-04-04 3/150 2026-04-05 07:48 by 544594351
[¿¼ÑÐ] 334Çóµ÷¼Á +8 ÔøÑöÖ® 2026-04-03 8/400 2026-04-04 11:16 by w_xuqing
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +11 ÎâèùÓ±£¡ 2026-04-03 11/550 2026-04-04 09:56 by ССÊ÷2024
[¿¼ÑÐ] ¿¼Ñе÷¼Á +8 ²»°®ºÈÒûÁÏ 2026-04-03 8/400 2026-04-03 16:40 by Mistake-J
[¿¼ÑÐ] 081200-11408-276ѧ˶Çóµ÷¼Á +6 ´Þwj 2026-04-02 6/300 2026-04-03 10:19 by À¶ÔÆË¼Óê
[¿¼ÑÐ] Ò»Ö¾Ô¸ÏÃÃÅ´óѧ»¯Ñ§¹¤³Ì£¨×¨Ë¶£©-Êý¶þÓ¢¶þ406·Ö-Çóµ÷¼Á +5 Ïô󻯹¤ 2026-04-01 5/250 2026-04-02 10:03 by jp9609
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û